A baby born with congenital rubella syndrome (CRS) is likely to have defects of major organs. These can include single or combined defects such as deafness, cataracts, microphthalmia (unnaturally small eyes), congenital glaucoma, congenital heart defects, microcephaly (abnormally small head and brain), meningoencephalitis (inflammation of the brain and its surrounding membrane), dermal erythropoiesis (production of red blood cells in the skin), thrombocytopenia (reduced platelet count) and developmental delay.
Management of babies with CRS is predominantly symptomatic with an emphasis on support for the parents and appropriate referrals in order to optimise the outcomes for the baby.
Babies with CRS are highly contagious and should be kept isolated from other babies and pregnant women.